Product NDC: | 41250-590 |
Proprietary Name: | pain and fever |
Non Proprietary Name: | acetaminophen |
Active Ingredient(s): | 160 mg/5mL & nbsp; acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41250-590 |
Labeler Name: | Meijer Distribution Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19930723 |
Package NDC: | 41250-590-10 |
Package Description: | 1 BOTTLE in 1 CARTON (41250-590-10) > 30 mL in 1 BOTTLE |
NDC Code | 41250-590-10 |
Proprietary Name | pain and fever |
Package Description | 1 BOTTLE in 1 CARTON (41250-590-10) > 30 mL in 1 BOTTLE |
Product NDC | 41250-590 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19930723 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Meijer Distribution Inc |
Substance Name | ACETAMINOPHEN |
Strength Number | 160 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |